BEUDAMED
    411 results · 21ms · Sources: EU EUDAMED, US FDA

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    BREATHID HP SYSTEM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707010722·CALIBRA 1ST MOLAR BANDS n.UL 24

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776163020·FLAT BLADE

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197047081·TC Semken Tissue Forceps 1x2 te...

    Scorpio

    FDA UDI
    Howmedica Osteonics Corp.·07613153992523·Posterior Stabilized Tibial Insert

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197047074·TC Semken Tissue Forceps 1x2 te...

    POLYTEL(R) APT MODEL: PWA-08-01

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CD LEYCOM 7 FR PRESSURE/VOLUME CATHETER (10 MM ELECTRODE SPACING) PRESSURE/VOLUME COMBINATION CATHETER WITH LUMEN

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM DE MEXICO S DE RL DE CV·Product code FPO·February 25, 2013

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·September 30, 2014

    NEXGEN LEGACY LPS ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·June 14, 2011

    KIWI VACUUM ASSISTED FETAL DELIVERY

    FDA Adverse Event
    Malfunction ·CLINICAL INNOVATIONS, INC.·Product code HDB·January 23, 2014

    ADULT DUAL HEATED EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZE·December 19, 2013

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 3, 2024

    CAPIOX®FX

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·February 19, 2026

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·May 22, 2015

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·June 9, 2022

    CAPIOX®FX

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·March 30, 2026

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 6, 2025

    CAPIOX FX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·August 25, 2021